Phase 3 Heart Disease Trial, Recruiting NCT06286878 Sponsor: University of Sao Paulo Condition: Heart Disease
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Phase 3 Heart Disease Trial, Recruiting

NCT06286878
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older (women who could become pregnant must have a negative pregnancy test result)
  • People already taking two blood-thinning medications together — aspirin plus a second type called an ADP receptor antagonist — as part of their usual care
  • People diagnosed with a heart attack (with or without a specific type called STEMI) within the last 7 days, using the most current medical definition of heart attack
  • People who have signed the official consent form agreeing to take part

Who may not be able to join:

  • People who have taken the diabetes medication pioglitazone within the last 24 months, or who have taken it for a total of 2 or more years at any point in their life
  • People who have taken the diabetes medication rosiglitazone within the last 12 months
  • People who have been regularly taking a type of diabetes medication called an SGLT2 inhibitor for more than 15 days in a row at the time of hospital admission
  • People who have been regularly taking oral steroid medications at higher doses for more than 30 consecutive days (confirm specific dose thresholds with trial site)
  • People with very high blood pressure at the time of enrolment (top number above 180 or bottom number above 100)
  • People diagnosed with Type 1 diabetes, a rare inherited form of diabetes called MODY, or diabetes caused by a hormonal condition, pancreatic surgery, medication, a tumour on the pancreas, or long-term pancreatic inflammation
  • People with a history of bladder cancer, or who have had radiation treatment to the lower abdomen or pelvis at any point
  • People who have had any other cancer in the past 5 years, except for certain non-melanoma skin cancers that were successfully treated
  • People with a long-term bladder condition or who have had 3 or more urinary tract infections in the past year
  • People with any condition the trial investigator believes would make it unsafe or unsuitable for them to complete the study — this includes certain heart complications, recurring dangerous heart rhythm problems, active cancer (other than a specific type of minor skin cancer), liver cirrhosis, chronic lung disease, or severe autoimmune disease
  • People who are pregnant or breastfeeding
  • People currently taking part in another clinical trial
  • People in septic shock or with severely uncontrolled blood sugar requiring insulin given through a drip at the time of enrolment
  • People with significantly elevated liver enzyme or bilirubin levels in their blood tests (confirm specific values with trial site)
  • People whose kidneys are not filtering blood well enough (below a specific threshold on a standard kidney function test), or who have had a kidney transplant
  • People known to have conditions that cause abnormal blood clotting or an unusually high platelet count
  • People with known blood disorders that cause the breakdown of red blood cells
  • People with certain abnormal blood count results at the time of enrolment, including low or very high haemoglobin, abnormal white blood cell counts, or platelet counts outside an accepted range (confirm specific values with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Jose JN Nicolu, University of Sao Paulo

Phone: +55 (11) 2661-5058

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
8 December 2021
Est. completion
30 July 2025

Where this trial is recruiting

🇧🇷 Brazil

Primary endpoints

Platelet aggregation using ADP

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov